P38P (p.Pro38Pro) variant of CALCB (P10092)
P38P (p.Pro38Pro) in CALCB (P10092) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.09 / 1. The record also includes population frequency data, published literature, and structural context.
P38P (p.Pro38Pro) variant details
- p.Pro38Pro
- rs1377497958
- gnomAD 11-15075088-G-A
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.0872
- CADD 0.92
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available
- Literature evidence available